Deatailed information for cohesin site CDBP00413192


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  • Basic information
  • CohesinDB ID: CDBP00413192
  • Locus: chr21-14070030-14074512
  • Data sourse: ENCSR000BLD, GSE206145-GSE177045, GSE72082, ENCSR000BLY, GSE105028, GSE25021, GSE131606, GSE67783, GSE86191, GSE206145-NatGen2015, GSE120943, ENCSR703TNG, GSE116344, ENCSR000EHW, GSE206145, ENCSR000ECE, ENCSR000EHX, ENCSR000BTQ, GSE111913, GSE68388, GSE83726, GSE38411
  • Cell type: MCF-7, H1-hESC, RPE, Fibroblast, HCT-116, Monocytes, RH4, DKO, RT-112, SK-N-SH, BCBL-1, HSPC, HuCC-T1, H9-hESC
  • DNA Sequence of binding site: UCSC hg38
  • Cohesin category
  • Peak occupancy ratio: 8% samples have this site.
  • Cell specificity (0: conserved, 1: cell type specific): 0.844
  • Subunit: SA1,Rad21,SMC1,SA2,Mau2,SMC3
  • CTCF binding site: CTCF CTCF motif: False
  • Genomic location: TSS,TES
  • 3D genome
  • TAD boundary: Boundary
  • Chromatin hubs: Hub
  • Hi-C loops: True Hi-ChIP loops: False ChIA-PET loops: True
  • Compartment: 37% Hi-C samples shows Compartment A
  • Cis-regulatory elements
  • Enhancer (Fantom5): non-Enhancer
  • Super enhancer (SEdb): False
  • Chromatin annotation: "15_Quies": 40%, "9_Het": 26%,
    Note: The percentage represent how many of the 127 Roadmap datasets show the indicated state (top 2).
  • Co-bound Transcriptional factors: RUNX1, TRP47, TRIM25, CBX1, FOXA2, MYCN, ZNF263, AGO1, ZFX, ZBTB48, WT1, FOXA1, TET2, ZBTB33, LEO1, ZNF28, ERG, YY1, RELA, CREBBP, OGG1, ATF3, MYC, CTCFL, RAD21, SP140, NFIB, ARNT, ZNF444, NRF1, CBFB, GRHL3, STAT3, MAX, TP63, NRIP1, PRDM14, AGO2, CHD1, MED1, NR3C1, TEAD1, TRIM28, RBM39, NR2F1, EZH2, ESR1, PKNOX1, OCA2, CTCF, RBM22, ZHX2, AR, RXR, EGR1, HEXIM1, TFIIIC, HSF1, BRD4, MAZ, AATF, SMC3, STAG1, TFAP2C
  • Target gene symbol (double-evidenced CRMs): SAMSN1
  • Function elements
  • Human SNPs: .
  • Number of somatic mutations (coding): 0
  • Number of somatic mutations (non-coding): 74
  • Related genes and loops

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